2018
DOI: 10.1021/acs.molpharmaceut.8b00661
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Targeted Imaging of VCAM-1 mRNA in a Mouse Model of Laser-Induced Choroidal Neovascularization Using Antisense Hairpin-DNA-Functionalized Gold-Nanoparticles

Abstract: Mouse laser-induced choroidal neovascularization (mouse LCNV) recapitulates the 'wet' form of human age-related macular degeneration (AMD). Vascular cell adhesion molecule-1 (VCAM-1) is a known inflammatory biomarker and it increases in the choroidal neovascular tissues characteristic of this experimental model. We have designed and constructed gold nanoparticles (AuNP) functionalized with hairpin-DNA that incorporates an anti-sense sequence complementary to VCAM-1 mRNA (AS-VCAM-1 hAuNP), and tested them as op… Show more

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Cited by 12 publications
(13 citation statements)
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“…AuNPs inhibited the phosphorylation of ERK1/2, Akt, and FAK in HUVECs [ 13 ]. Optical coherence tomography (OCT)-assisted CNV volume measurement at all time points showed a significant reduction in lesion size in the group that received an intravenous injection of gold nanoparticles when compared with controls [ 11 , 14 ]. Most notably, metal nanoparticles with diameters of 20 and 80 nm (0.0065 µg/mL 20 nm AuNPs, 0.4 µg/mL 80 nm AuNPs, 0.0035 µg/mL 20 nm AgNPs, and 0.22 µg/mL 80 nm AgNPs) are toxic to photoreceptor cells in vitro [ 15 ].…”
Section: Retinopathymentioning
confidence: 99%
“…AuNPs inhibited the phosphorylation of ERK1/2, Akt, and FAK in HUVECs [ 13 ]. Optical coherence tomography (OCT)-assisted CNV volume measurement at all time points showed a significant reduction in lesion size in the group that received an intravenous injection of gold nanoparticles when compared with controls [ 11 , 14 ]. Most notably, metal nanoparticles with diameters of 20 and 80 nm (0.0065 µg/mL 20 nm AuNPs, 0.4 µg/mL 80 nm AuNPs, 0.0035 µg/mL 20 nm AgNPs, and 0.22 µg/mL 80 nm AgNPs) are toxic to photoreceptor cells in vitro [ 15 ].…”
Section: Retinopathymentioning
confidence: 99%
“…Furthermore, their mass production is facilitated by their ease of synthesis and controlled sizes. of utmost importance are the capacity of aunPs to carry nucleic acid payloads and their unique role in PTT (10,11). The current review divided aunPs into 3 groups: Simple drug-carrying aunPs, simple nucleic acid-carrying aunPs and targeted aunPs.…”
Section: Resultsmentioning
confidence: 99%
“…Gold nPs (aunPs) have received increasing attention as drug delivery vehicles for cancer therapeutics as they can be engineered to obviate drug insolubility, carry nucleic acid payloads for gene therapy, target specific tumor cell lines, modulate drug release and amplify photothermal therapy (PTT) (10,11). The development of gene therapy has generated increasing interest in the potential of aunPs to deliver therapeutic nucleic acid payloads (10,11). aunPs have been designed to carry p53, vascular cell adhesion molecule-1 and other mrnas (10,11).…”
Section: Gold Nanoparticle-mediated Delivery Of Paclitaxel and Nucleimentioning
confidence: 99%
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“…An in vivo model of human “wet” AMD is laser-induced choroidal neovascularization (mouse LCNV) mouse, in which the inflammatory biomarker vascular cell adhesion molecule-1 (VCAM-1) is highly expressed. Gold nanoparticles functionalized with anti-sense DNA complementary to VCAM-1 mRNA were developed by Uddin et al, who aimed to detect this molecule, thus assessing the occurrence of oxidative stress [ 147 ]. The fluorescence in-situ hybridization (FISH) technique was used to perform photothermal-optical coherence tomography (PT-OCT) involving a fluorescent probe (Alexafluor-647) bonded to 3′ end of anti-sense DNA in order to highlight its interaction with the target mRNA.…”
Section: Fluorescent Nanosystems In Ocular Applicationmentioning
confidence: 99%